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BMC Medical Genetics
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101 Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population.
102 Adult case of partial trisomy 9q.
103 Leptin receptor (LEPR) SNP polymorphisms in HELLP syndrome patients determined by quantitative real-time PCR and melting curve analysis.
104 Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study.
105 A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family.
106 Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy.
107 Loss of balancing selection in the beta S globin locus.
108 A novel germline PALB2 deletion in Polish breast and ovarian cancer patients.
109 Frequency of FD in male and female haemodialysis patients in Spain.
110 Genetic selection? A study of individual variation in the enzymes of folate metabolism.
111 Toll-like receptor 2 gene polymorphisms, pulmonary tuberculosis, and natural killer cell counts.
112 Haplotypes of intron 4 of the estrogen receptor alpha gene and hip fractures: a replication study in Caucasians.
113 Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.
114 Modeling complex genetic and environmental influences on comorbid bipolar disorder with tobacco use disorder.
115 The G-Protein beta 3 subunit 825 TT genotype is associated with epigastric pain syndrome-like dyspepsia.
116 Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS).
117 Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population.
118 CXCR1 and SLC11A1 polymorphisms affect susceptibility to cutaneous leishmaniasis in Brazil: a case-control and family-based study.
119 Sex-specific effects of scavenger receptor class B type 1 (SR-BI) gene variants on serum lipid levels and hepatic gene expression.
120 Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis.
 
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